A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116373



Internal ID18922638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:675498..675670hg38UCSC Ensembl
Outerchr6:675498..675670hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3249n106
Supporting Variantsnssv3955512
SamplesKWS1
Known GenesEXOC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116373
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer